Subepithelial autoimmune blistering dermatoses: Clinical features and diagnosis

Carmen M. Montagnon; Stanislav N. Tolkachjov; Dedee F. Murrell; Michael J. Camilleri; Julia S. Lehman

doi:10.1016/j.jaad.2020.11.076

Subepithelial autoimmune blistering dermatoses: Clinical features and diagnosis

Carmen M. Montagnon, Stanislav N. Tolkachjov, Dedee F. Murrell, Michael J. Camilleri, Julia S. Lehman

Dermatology

Research output: Contribution to journal › Review article › peer-review

Abstract

Subepithelial autoimmune blistering dermatoses are a group of rare skin disorders that are characterized by the disruption of the dermal-epidermal junction through the action of autoantibodies. The third article in this continuing medical education series explores the background, epidemiology, clinical features, and diagnostic criteria of each of the major subepithelial autoimmune blistering dermatoses, including bullous pemphigoid, pemphigoid gestationis, lichen planus pemphigoides, mucous membrane pemphigoid, linear IgA bullous dermatosis, and dermatitis herpetiformis.

Original language	English (US)
Pages (from-to)	1-14
Number of pages	14
Journal	Journal of the American Academy of Dermatology
Volume	85
Issue number	1
DOIs	https://doi.org/10.1016/j.jaad.2020.11.076
State	Published - Jul 2021

Keywords

bullous eruption of systemic lupus erythematosus
bullous pemphigoid
dermatitis herpetiformis
drug-induced bullous pemphigoid
epidermolysis bullosa acquisita
herpes gestationis
lichen planus pemphigoides
linear IgA bullous dermatosis
mucous membrane pemphigoid

ASJC Scopus subject areas

Dermatology

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10.1016/j.jaad.2020.11.076

Cite this

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title = "Subepithelial autoimmune blistering dermatoses: Clinical features and diagnosis",

abstract = "Subepithelial autoimmune blistering dermatoses are a group of rare skin disorders that are characterized by the disruption of the dermal-epidermal junction through the action of autoantibodies. The third article in this continuing medical education series explores the background, epidemiology, clinical features, and diagnostic criteria of each of the major subepithelial autoimmune blistering dermatoses, including bullous pemphigoid, pemphigoid gestationis, lichen planus pemphigoides, mucous membrane pemphigoid, linear IgA bullous dermatosis, and dermatitis herpetiformis.",

keywords = "bullous eruption of systemic lupus erythematosus, bullous pemphigoid, dermatitis herpetiformis, drug-induced bullous pemphigoid, epidermolysis bullosa acquisita, herpes gestationis, lichen planus pemphigoides, linear IgA bullous dermatosis, mucous membrane pemphigoid",

author = "Montagnon, {Carmen M.} and Tolkachjov, {Stanislav N.} and Murrell, {Dedee F.} and Camilleri, {Michael J.} and Lehman, {Julia S.}",

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AU - Tolkachjov, Stanislav N.

AU - Murrell, Dedee F.

AU - Camilleri, Michael J.

AU - Lehman, Julia S.

PY - 2021/7

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AB - Subepithelial autoimmune blistering dermatoses are a group of rare skin disorders that are characterized by the disruption of the dermal-epidermal junction through the action of autoantibodies. The third article in this continuing medical education series explores the background, epidemiology, clinical features, and diagnostic criteria of each of the major subepithelial autoimmune blistering dermatoses, including bullous pemphigoid, pemphigoid gestationis, lichen planus pemphigoides, mucous membrane pemphigoid, linear IgA bullous dermatosis, and dermatitis herpetiformis.

KW - bullous eruption of systemic lupus erythematosus

KW - bullous pemphigoid

KW - dermatitis herpetiformis

KW - drug-induced bullous pemphigoid

KW - epidermolysis bullosa acquisita

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KW - lichen planus pemphigoides

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Subepithelial autoimmune blistering dermatoses: Clinical features and diagnosis

Abstract

Keywords

ASJC Scopus subject areas

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